Works matching IS 09646906 AND DT 2003 AND VI 12 AND IP 19
Results: 15
Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased α7 integrin, utrophin and associated glycoproteins.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2467, doi. 10.1093/hmg/ddg264
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- Article
Gene expression changes presage neurodegeneration in a Drosophila model of Parkinson's disease.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2457, doi. 10.1093/hmg/ddg265
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- Article
Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2503, doi. 10.1093/hmg/ddg266
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- Article
Increased expression of the glial glutamate transporter EAAT2 modulates excitotoxicity and delays the onset but not the outcome of ALS in mice.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2519, doi. 10.1093/hmg/ddg267
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- Article
Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2547, doi. 10.1093/hmg/ddg263
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- Article
X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2559, doi. 10.1093/hmg/ddg268
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- Article
Association of TNF-α promoter polymorphisms with the clearance of hepatitis B virus infection.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2541, doi. 10.1093/hmg/ddg262
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- Article
Valproic acid increases the SMN2 protein level: a well-known drug as a potential therapy for spinal muscular atrophy.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2481, doi. 10.1093/hmg/ddg256
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- Article
A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2533, doi. 10.1093/hmg/ddg255
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- Article
Significant linkage to migraine with aura on chromosome 11q24.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2511, doi. 10.1093/hmg/ddg252
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A unification of mosaic structures in the human genome.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2411, doi. 10.1093/hmg/ddg251
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- Article
Lowe syndrome protein OCRL1 interacts with Rac GTPase in the trans-Golgi network.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2449, doi. 10.1093/hmg/ddg250
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- Article
Identification of SATB2 as the cleft palate gene on 2q32–q33.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2491, doi. 10.1093/hmg/ddg248
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- Article
LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2417, doi. 10.1093/hmg/ddg247
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- Article
Complexin II is essential for normal neurological function in mice.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2431, doi. 10.1093/hmg/ddg249
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- Article